Variant report
Variant | rs56302757 |
---|---|
Chromosome Location | chr6:64511208-64511209 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000112245 | Chromatin interaction |
ENSG00000266680 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11753940 | 0.87[ASN][1000 genomes] |
rs11754041 | 0.84[ASN][1000 genomes] |
rs11754728 | 0.83[ASN][1000 genomes] |
rs11755371 | 0.81[ASN][1000 genomes] |
rs11755458 | 0.88[ASN][1000 genomes] |
rs11755460 | 0.88[ASN][1000 genomes] |
rs11756799 | 0.84[ASN][1000 genomes] |
rs11756833 | 0.84[ASN][1000 genomes] |
rs11757713 | 0.87[ASN][1000 genomes] |
rs11757834 | 0.90[ASN][1000 genomes] |
rs11758365 | 0.88[ASN][1000 genomes] |
rs11758738 | 0.84[ASN][1000 genomes] |
rs1197983 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1333096 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1333097 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1572115 | 0.93[ASN][1000 genomes] |
rs1681939 | 0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs16894562 | 0.90[ASN][1000 genomes] |
rs1905593 | 0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1999579 | 0.83[ASN][1000 genomes] |
rs2008452 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34254442 | 0.90[ASN][1000 genomes] |
rs3757350 | 0.84[ASN][1000 genomes] |
rs3778647 | 0.82[ASN][1000 genomes] |
rs3778648 | 0.84[ASN][1000 genomes] |
rs3800491 | 0.84[ASN][1000 genomes] |
rs3800492 | 0.84[ASN][1000 genomes] |
rs3800493 | 0.84[ASN][1000 genomes] |
rs3823446 | 0.84[ASN][1000 genomes] |
rs41271589 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs52546 | 0.80[ASN][1000 genomes] |
rs55678650 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs55802833 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs56008921 | 0.83[ASN][1000 genomes] |
rs56088368 | 0.83[ASN][1000 genomes] |
rs56172936 | 0.82[ASN][1000 genomes] |
rs56300303 | 0.84[ASN][1000 genomes] |
rs56360535 | 0.93[ASN][1000 genomes] |
rs57217151 | 0.87[ASN][1000 genomes] |
rs57280061 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs57305989 | 0.90[ASN][1000 genomes] |
rs57319124 | 0.81[ASN][1000 genomes] |
rs57657484 | 0.83[ASN][1000 genomes] |
rs57888259 | 0.86[ASN][1000 genomes] |
rs57891105 | 0.80[ASN][1000 genomes] |
rs58198138 | 0.90[ASN][1000 genomes] |
rs58247688 | 0.88[ASN][1000 genomes] |
rs58531869 | 0.86[ASN][1000 genomes] |
rs58669837 | 0.83[ASN][1000 genomes] |
rs59217667 | 0.83[ASN][1000 genomes] |
rs59674359 | 0.84[ASN][1000 genomes] |
rs60289981 | 0.83[ASN][1000 genomes] |
rs60564402 | 0.81[ASN][1000 genomes] |
rs60622008 | 0.83[ASN][1000 genomes] |
rs60694786 | 0.83[ASN][1000 genomes] |
rs60949185 | 0.80[ASN][1000 genomes] |
rs61079290 | 0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs61094361 | 0.88[ASN][1000 genomes] |
rs61268055 | 0.86[ASN][1000 genomes] |
rs61369019 | 0.84[ASN][1000 genomes] |
rs61606312 | 0.88[ASN][1000 genomes] |
rs66462731 | 0.90[ASN][1000 genomes] |
rs66481681 | 0.88[ASN][1000 genomes] |
rs66520187 | 0.84[ASN][1000 genomes] |
rs66589841 | 0.88[ASN][1000 genomes] |
rs66752943 | 0.88[ASN][1000 genomes] |
rs66804407 | 0.88[ASN][1000 genomes] |
rs66882701 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs66960758 | 0.83[ASN][1000 genomes] |
rs66973400 | 0.88[ASN][1000 genomes] |
rs67044231 | 0.88[ASN][1000 genomes] |
rs67050101 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs67069403 | 0.88[ASN][1000 genomes] |
rs67169857 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs67342772 | 0.84[ASN][1000 genomes] |
rs67362704 | 0.88[ASN][1000 genomes] |
rs67632239 | 0.88[ASN][1000 genomes] |
rs67632720 | 0.88[ASN][1000 genomes] |
rs67674014 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs67722441 | 0.88[ASN][1000 genomes] |
rs67725686 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67727731 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs67733371 | 0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67856629 | 0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs67890600 | 0.88[ASN][1000 genomes] |
rs67904296 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs67935772 | 0.88[ASN][1000 genomes] |
rs67939679 | 0.90[ASN][1000 genomes] |
rs67958548 | 0.90[ASN][1000 genomes] |
rs67959580 | 0.88[ASN][1000 genomes] |
rs68128834 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs68132675 | 0.88[ASN][1000 genomes] |
rs68177305 | 0.88[ASN][1000 genomes] |
rs6911092 | 0.84[ASN][1000 genomes] |
rs6933866 | 0.90[ASN][1000 genomes] |
rs72884634 | 0.84[ASN][1000 genomes] |
rs72884640 | 0.84[ASN][1000 genomes] |
rs72886339 | 0.88[ASN][1000 genomes] |
rs72886350 | 0.88[ASN][1000 genomes] |
rs72888273 | 0.83[ASN][1000 genomes] |
rs72890149 | 0.83[ASN][1000 genomes] |
rs7758431 | 0.88[ASN][1000 genomes] |
rs958324 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830674 | chr6:64355412-64535801 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1024367 | chr6:64453493-64615908 | Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | esv1798215 | chr6:64487748-64544220 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:64485200-64514400 | Weak transcription | Adipose Nuclei | Adipose |
2 | chr6:64497000-64514400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr6:64505800-64512800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
4 | chr6:64506200-64514400 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
5 | chr6:64509800-64514600 | Weak transcription | Stomach Mucosa | stomach |
6 | chr6:64510000-64512800 | Weak transcription | NHDF-Ad | bronchial |
7 | chr6:64510000-64514200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
8 | chr6:64510200-64512600 | Weak transcription | Primary monocytes fromperipheralblood | blood |
9 | chr6:64511000-64511600 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
10 | chr6:64511000-64514400 | Weak transcription | Liver | Liver |